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Eclevar and Unither entered into an agreement to collect RWE on ORL medical devices for rare disease patients

Paris, September 10, 2024 – Eclevar MedTech, a leading Contract Research Organization (CRO) specializing in medical devices and in vitro diagnostics, is proud to announce its selection by Unither Pharmaceuticals to lead their upcoming clinical studies on their medical devices. This collaboration marks a significant milestone in the partnership between the two companies, aimed at enhancing innovation and efficiency in healthcare.

Eclevar MedTech and RegenLab entered into an agreement to conduct all upcoming PMCF studies for chronic diabetic foot ulcer devices

Paris, October 03, 2024 –Eclevar MedTech, a leading european contract research organization (CRO) specializing in medical devices, proudly announces its colleboration with by RegenLab (Swiss manufacturer of medical device) to lead their upcoming clinical studies on their innovative medical devices in wound care. This partnership marks a crucial step in the collaboration between the two companies, aiming to enhance innovation and make products of RegenLab compliant to the european requirement of the MDR 745/2017

Eclevar MedTech and ASAHI INTECC have entered into an agreement to provide consulting expertise in clinical evaluation and post-market clinical follow-up (PMCF) strategies for a Class III vascular catheter device

Paris, October 21, 2024 – Eclevar MedTech, a leading european contract research organization (CRO) specializing in medical devices, proudly announces its colleboration with by Asahi intecc (Japan manufacturer of medical device) to provide consulting expertise in clinical evaluation and post-market clinical follow-up (PMCF) strategies in interventional cardiovascular area. This partnership marks a crucial step in the collaboration between the two companies, aiming to enhance innovation and make products of Asahi Intecc compliant to the european requirement of the MDR 745/2017.

GENTELL reaches an agreement with ECLEVAR MedTech for consulting services in clinical evaluation and PMCF strategy, addressing CER and validation requirements.

Paris, October 07, 2024 – Eclevar MedTech, a leading european contract research organization (CRO) specializing in medical devices, proudly announces its colleboration with GENTELL (US manufacturer of medical device) to provide consulting expertise in clinical evaluation and post-market clinical follow-up (PMCF) strategies in wound care dressings and related products. This partnership marks a crucial step in the collaboration between the two companies, aiming to enhance innovation and make products of GENTELL compliant to the european requirement of the MDR 745/2017.

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